Search results for "Ligo"

showing 10 items of 1427 documents

Noncovalent Saccharide Recognition by Means of a Tetrakis(bile acid)-Porphyrin Conjugate: Selectivity, Cooperation, and Stability

2010

Molecular recognition of Glu, Glc 2 -Glc 6 and Mal 3 by a tetrakis(bile acid)―porphyrin conjugate has been studied by using ESI-FTICR mass spectrometry. The bile acid conjugate was observed to form 1:1 noncovalent complexes with saccharides. The conjugate was found to have size-selectivity towards saccharides with three or more glucose residues. The Glc 3 and Glc 4 also formed kinetically the most stable complexes. The electron capture dissociation (ECD) experiments revealed that in complexation of an oligosaccharide three glucose residues interact with the bile acid conjugate, whereas additional glucose residues are susceptible to fragmentation. The ECD results also showed the significance…

chemistry.chemical_classificationElectron-capture dissociationBile acidmedicine.drug_classStereochemistryOrganic ChemistryOligosaccharidePorphyrinchemistry.chemical_compoundMolecular recognitionchemistryAldosemedicineNon-covalent interactionsPhysical and Theoretical ChemistryConjugateEuropean Journal of Organic Chemistry
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2-Chloro/phenyl-7-arylimino-6,6-dimethylcyclopenta[b]pyridylnickel chlorides: Synthesis, characterization and ethylene oligomerization

2017

Abstract 2-Chloro/phenyl-7-arylimino-6,6-dimethylcyclopenta[b]pyridylnickel chlorides (Ni1–Ni8) were synthesized from the respective ligands L1–L8 and characterized. Upon activation with either methylaluminoxane (MAO) or ethylaluminium sesquichloride (EASC), they show high catalytic activity of up to 10.84 × 106 g(oligomer) mol− 1(Ni) h− 1 in ethylene oligomerization. The products range from butenes to dodecenes for Ni1–Ni4, but are limited to butenes and hexenes in the case of Ni5–Ni8. DFT calculations indicate that the Ni C bond length in the model alkyl complexes depends both on the nature of the substituents at the heterocycles and the kind of the alkyl group, shedding some light on the…

chemistry.chemical_classificationEthylene010405 organic chemistryethylene oligomerizationProcess Chemistry and TechnologyMethylaluminoxaneGeneral ChemistryPolyethylene010402 general chemistry01 natural sciencesOligomerMedicinal chemistryCatalysis0104 chemical sciencesCatalysisBond lengthnickel precatalystchemistry.chemical_compoundchemistrysubstituent influenceEthylaluminium sesquichlorideOrganic chemistry7-Aryliminocyclopenta[b]pyridineAlkylCatalysis Communications
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Xyloglucan-derived oligosaccharides induce ethylene synthesis in persimmon (Diospyros kaki L.) fruit

1998

In this work the effect of injection of xyloglucan-derived oligosaccharides (XGOs) into whole persimmon (Diospyros kaki L.) fruits on ethylene biosynthesis was investigated. Fruits collected during different ripening stages produced low levels of ethylene without a climacteric-like peak. Pretreatment of these fruits with 10 cm 3 C 2 H4 m -3 for 8 h stimulated little or no endogenous ethylene production. However, when persimmon fruits were injected with a mixture of XGOs a burst in ethylene production was observed compared with water-injected control fruits or fruits injected with different monosaccharide solutions. In order to study the influence of oligosaccharide structure and fruit ripen…

chemistry.chemical_classificationEthylenebiologyPhysiologyfood and beveragesDiospyros kakiRipeningPlant ScienceDiospyrosOligosaccharidebiology.organism_classificationXyloglucanchemistry.chemical_compoundchemistryBiochemistryFood scienceEbenaceaeFruit treeJournal of Experimental Botany
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Pentadecamer 2,5-Dipropoxy-1,4-phenylenevinylene

2002

The conjugated, all-(E)-configured pentadecamer 2,5-dipropoxy-1,4-phenylenevinylene 1j was prepared by a multistep synthesis on the basis of hydroquinone. The procedure consists of a general method for the repetitive extension of oligo(phenylenvinylene) chains by two styryl units (7a ⇄ 10 ⇄ 12 ⇄ 14). The relatively rigid oligomer 1j represents a molecular wire of about 100 A. The absorption of 1j provides a proof for the convergence theory for electronic properties of conjugated oligomers with increasing number of repeat units. The corresponding conjugated polymer 1p with the same substitution matches the values which were extrapolated from the oligomer series 1a−1j. (© Wiley-VCH Verlag Gmb…

chemistry.chemical_classificationGeneral methodHydroquinoneOrganic ChemistryPolymerConjugated systemOligomerchemistry.chemical_compoundMolecular wirechemistryPolymer chemistryPhysical and Theoretical ChemistryAbsorption (chemistry)Electronic propertiesEuropean Journal of Organic Chemistry
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Hemocyanin from the keyhole limpetMegathura crenulata(KLH) carries a novel type of N-glycans with Gal(β1-6)Man-motifs

2002

Keyhole limpet (Megathura crenulata) hemocyanin (KLH), an extracellular respiratory protein, is widely used as hapten carrier and immune stimulant. Although it is generally accepted that the sugar constituents of this glycoprotein are likely to be implicated in the antigenicity and biomedical properties of KLH, knowledge of its carbohydrate structure is still limited. Therefore, we have investigated the N-linked oligosaccharides of KLH. Glycan chains were enzymatically liberated from tryptic glycopeptides, pyridylaminated and separated by two-dimensional HPLC. Only neutral oligosaccharides were obtained and characterized by carbohydrate constituent and methylation analyses, MALDI-TOF-MS, ES…

chemistry.chemical_classificationGlycanAntigenicitybiologychemical and pharmacologic phenomenaOligosaccharideMegathura crenulatabiology.organism_classificationBiochemistryRespiratory proteinchemistryBiochemistryExoglycosidasebiology.proteinGlycoproteinHaptenEuropean Journal of Biochemistry
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N-glycosylation efficiency is determined by the distance to the C-terminus and the amino acid preceding an Asn-Ser-Thr sequon

2010

N-glycosylation is the most common and versatile protein modification. In eukaryotic cells, this modification is catalyzed cotranslationally by the enzyme oligosaccharyltransferase, which targets the β-amide of the asparagine in an Asn-Xaa-Ser/Thr consensus sequon (where Xaa is any amino acid but proline) in nascent proteins as they enter the endoplasmic reticulum. Because modification of the glycosylation acceptor site on membrane proteins occurs in a compartment-specific manner, the presence of glycosylation is used to indicate membrane protein topology. Moreover, glycosylation sites can be added to gain topological information. In this study, we explored the determinants of N-glycosylati…

chemistry.chemical_classificationGlycosylationbiologyOligosaccharyltransferaseSequonBiochemistryAmino acidcarbohydrates (lipids)chemistry.chemical_compoundN-linked glycosylationBiochemistrychemistryO-linked glycosylationbiology.proteinlipids (amino acids peptides and proteins)AsparagineGlycoproteinMolecular BiologyProtein Science
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Identification of the reaction products of (2'-5')oligoadenylate synthetase in the marine sponge.

1998

Previously we reported on the presence of a high (2'-5')oligoadenylate synthetase activity in the marine sponge Geodia cydonium [Kuusksalu, A., Pihlak, A., Muller, W. E. G. & Kelve, M. (1995) Eur. J. Biochem. 232, 351-357]. The presence of (2'-5')oligoadenylates [(2'-5')A] in crude sponge extract was shown by radioimmunoassay and by their HPLC comigration with authentic (2'-5')A oligomers. In addition, the sponge (2'-5')oligoadenylates displayed biological activity, as determined by inhibition studies of protein biosynthesis in rabbit reticulocyte lysate. In the present study individual (2'-5')oligoadenylates synthesized by sponge enzyme were separated by HPLC. The exact composition of ever…

chemistry.chemical_classificationMagnetic Resonance Spectroscopy2'-5'-OligoadenylateOligonucleotideBiological activityNuclear magnetic resonance spectroscopyBiologyBiochemistryPoriferaEnzymemedicine.anatomical_structureBiochemistrychemistryReticulocyteSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationPhosphodiester bondProtein biosynthesismedicine2'5'-Oligoadenylate SynthetaseAnimalsChromatography High Pressure LiquidEuropean journal of biochemistry
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Degradable cationic nanohydrogel particles for stimuli-responsive release of siRNA.

2014

Well-defined nanogels have become quite attractive as safe and stable carriers for siRNA delivery. However, to avoid nanoparticle accumulation, they need to provide a stimuli-responsive degradation mechanism that can be activated at the payload's site of action. In this work, the synthetic concept for generating well-defined nanohydrogel particles is extended to incorporate disulfide cross-linkers into a cationic nanonetwork for redox-triggered release of oligonucleotide payload as well as nanoparticle degradation under reductive conditions of the cytoplasm. Therefore, a novel disulfide-modified spermine cross-linker is designed that both allows disassembly of the nanogel as well as removal…

chemistry.chemical_classificationMagnetic Resonance SpectroscopyPolymers and PlasticsChemistryOligonucleotideSpermidineOrganic ChemistryCationic polymerizationNanoparticleNanogelsFluorescence correlation spectroscopyHydrogelsPolymerPolyethylene GlycolsNanotoxicologyCationsAgarose gel electrophoresisMaterials ChemistryBiophysicsPolyethyleneimineDisulfidesRNA Small InterferingNanogelMacromolecular rapid communications
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Relationship between structure and electroluminescence of oligo(p-phenylenevinylene)s

1998

The preparation of LEDs with poly(p-phenylenevinylene) (PPV) as emitting material is well established, However, due to the presence of a distribution of conjugated chain lengths in the polymer, systematic investigations of the electroluminescence with polymeric materials are difficult, as far as the optical emission is concerned. We are studying the relationship between structural variation of substituted oligo(p-phenylenevinylene)s and their electroluminescent behaviour using a series of distyrylbenzenes with a variety of substituents in order to investigate their influence on the electroluminescence (EL). Furthermore, we synthesized a homologous series of monodisperse oligo(2,5-dipropoxy-…

chemistry.chemical_classificationMaterials sciencePhotoluminescenceOrganic ChemistryPolymerConjugated systemElectroluminescencePhotochemistryOligomerAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsInorganic Chemistrychemistry.chemical_compoundHomologous seriesMonomerchemistryPolymer chemistryPolystyreneElectrical and Electronic EngineeringPhysical and Theoretical ChemistrySpectroscopyOptical Materials
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A Precursor Route to Supramolecular Oligo(p-phenylene terephthalamide) Block Copolymers

2008

New soluble precursors for the step-wise synthesis of oligo(p-phenylene terephthalamide) block copolymers are described. Kevlar-like aramide oligomers up to the hexamer (six phenyl groups) were prepared in a polymer-analogous manner. Activating the carboxylic-acid-carrying oligomers as carbonyl chlorides while reversibly transforming the aromatic amides into imidoyl chlorides gave access to soluble precursors. The dimer and tetramer precursor were prepared and used in block copolymer synthesis. Single-crystal XRD confirmed the structure of the dimer precursor. Above a critical rod length, the Kevlar-like rod-coil block copolymers show strong aggregation in non-polar solvents such as chlorof…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsDimerOrganic ChemistryRandom hexamerOligomerSupramolecular polymerschemistry.chemical_compoundchemistryTetramerPhenylenePolymer chemistryMaterials ChemistryCopolymerSelf-assemblyMacromolecular Rapid Communications
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